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Thermo Fisher
gene exp dock7 hs00290630 m1 Gene Exp Dock7 Hs00290630 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 89/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/dock7+gene/pmc05476422-805-42-18?v=Thermo+Fisher Average 89 stars, based on 1 article reviews
gene exp dock7 hs00290630 m1 - by Bioz Stars,
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Full length Clone DNA of Human dedicator of cytokinesis 7
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Thermo Fisher
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Thermo Fisher
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MedGen Inc
dock7 gene ![]() Dock7 Gene, supplied by MedGen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/dock7+gene/pmc04727555-388-19-4?v=MedGen+Inc Average 90 stars, based on 1 article reviews
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Dock7 KN2 0 Mouse gene knockout kit via CRISPR non homology mediated
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Image Search Results
Journal: bioRxiv
Article Title: Deletion of Dock7 Exons 3 and 4 Results in Reduced Trabecular Microarchitecture and a Decrease in Mineralization
doi: 10.64898/2025.12.31.696872
Figure Lengend Snippet: (A) Schematic of the Dock7 wild type (+) and Dock7 exons 3–4 deletion ( Dock7-em2) transgenic allele. Image created with BioRender.com. (B) Predicted translation of the Dock7+ and Dock7-em2 alleles. Image created with BioRender.com. (C) Representative images of Dock7 +/+ , Dock7 +/em2 , and Dock7 em2/em2 mice.
Article Snippet: Dock7 exons 3–4 levels were quantified using a TaqMan gene expression assay containing primers that span across Dock7 exons 3–4 (
Techniques: Transgenic Assay
Journal: bioRxiv
Article Title: Deletion of Dock7 Exons 3 and 4 Results in Reduced Trabecular Microarchitecture and a Decrease in Mineralization
doi: 10.64898/2025.12.31.696872
Figure Lengend Snippet: (A) RNA expression of Dock7 exons 3–4, exons 11–12, and exons 34–35 was analyzed in BMSCs differentiated for 7 days in osteogenic media. Points represent individual replicates for all 3 experiments. (B) Quantitative protein analysis of DOCK7 peptides was performed by mass spectrometry in BMSC isolated from Dock7 +/+ and Dock7 em2/em2 mice. N=2 mice/group. Points represent replicates from all mice. (C) DOCK7 peptides were detected by mass spectrometry and used to quantify total DOCK7 levels. High confidence (green), medium confidence (yellow), and low confidence (red) DOCK7 peptides are indicated. The protein sequence corresponding to DOCK7 exons 3–4, the DHR1 domain, and the DHR2 domain is underlined and labeled.
Article Snippet: Dock7 exons 3–4 levels were quantified using a TaqMan gene expression assay containing primers that span across Dock7 exons 3–4 (
Techniques: RNA Expression, Mass Spectrometry, Isolation, Sequencing, Labeling
Journal: bioRxiv
Article Title: Deletion of Dock7 Exons 3 and 4 Results in Reduced Trabecular Microarchitecture and a Decrease in Mineralization
doi: 10.64898/2025.12.31.696872
Figure Lengend Snippet: Body composition was measured by DXA analysis in male and female Dock7 em2/em2 mice and compared to Dock7 +/+ control mice. Data was analyzed by 2-way ANOVA and Holm-Šídák’s test for post-hoc analysis. N=14–15 mice/group. Points represent each mouse.
Article Snippet: Dock7 exons 3–4 levels were quantified using a TaqMan gene expression assay containing primers that span across Dock7 exons 3–4 (
Techniques: Control
Journal: bioRxiv
Article Title: Deletion of Dock7 Exons 3 and 4 Results in Reduced Trabecular Microarchitecture and a Decrease in Mineralization
doi: 10.64898/2025.12.31.696872
Figure Lengend Snippet: Osteogenic differentiation was assessed in BMSCs that were isolated from Dock7 +/+ and Dock7 em2/em2 mice after 7 days of osteogenic differentiation. (A) Representative image of von Kossa and alkaline phosphatase staining. (B) Expression of the osteoblast-related genes Runx2 , AlpI , and Bglap . Points represent individual replicates for all 3 experiments.
Article Snippet: Dock7 exons 3–4 levels were quantified using a TaqMan gene expression assay containing primers that span across Dock7 exons 3–4 (
Techniques: Isolation, Staining, Expressing
Journal: Journal of Cellular and Molecular Medicine
Article Title: Association of the variants and haplotypes in the DOCK 7, PCSK 9 and GALNT 2 genes and the risk of hyperlipidaemia
doi: 10.1111/jcmm.12713
Figure Lengend Snippet: The association between the DOCK7 , PCSK9 and GALNT2 polymorphisms with hypercholesterolaemia
Article Snippet: DOCK7 (gene ID: 85440,
Techniques:
Journal: Journal of Cellular and Molecular Medicine
Article Title: Association of the variants and haplotypes in the DOCK 7, PCSK 9 and GALNT 2 genes and the risk of hyperlipidaemia
doi: 10.1111/jcmm.12713
Figure Lengend Snippet: The association between the DOCK7 , PCSK9 and GALNT2 polymorphisms with hypertriglyceridaemia
Article Snippet: DOCK7 (gene ID: 85440,
Techniques:
Journal: Journal of Cellular and Molecular Medicine
Article Title: Association of the variants and haplotypes in the DOCK 7, PCSK 9 and GALNT 2 genes and the risk of hyperlipidaemia
doi: 10.1111/jcmm.12713
Figure Lengend Snippet: Association between the genotypes of DOCK7 , PCSK9 and GALNT2 SNPs and serum lipid levels in the hypercholesterolaemic and non‐hypercholesterolaemic individuals
Article Snippet: DOCK7 (gene ID: 85440,
Techniques:
Journal: Journal of Cellular and Molecular Medicine
Article Title: Association of the variants and haplotypes in the DOCK 7, PCSK 9 and GALNT 2 genes and the risk of hyperlipidaemia
doi: 10.1111/jcmm.12713
Figure Lengend Snippet: Association between the genotypes of DOCK7 , PCSK9 and GALNT2 SNPs and serum lipid levels in the hypertriglyceridaemic and non‐hypertriglyceridaemic individuals
Article Snippet: DOCK7 (gene ID: 85440,
Techniques:
Journal: Journal of Cellular and Molecular Medicine
Article Title: Association of the variants and haplotypes in the DOCK 7, PCSK 9 and GALNT 2 genes and the risk of hyperlipidaemia
doi: 10.1111/jcmm.12713
Figure Lengend Snippet: The association between the DOCK7, PCSK9 and GALNT2 haplotypes and hypercholesterolaemia/hypertriglyceridaemia
Article Snippet: DOCK7 (gene ID: 85440,
Techniques: Control